Visualization systems, instruments and methods of using the same in spinal decompression procedures

ABSTRACT

A method for positioning a treatment instrument in a subject involves positioning a tissue protector of a visualization instrument in an epidural space of the subject. The tissue protector is viewed and positioned in the epidural space using fluoroscopy. A treatment instrument between a first vertebra and a second vertebra and while viewing the tissue protector positioned in the epidural space. A decompression procedure is performed using the treatment instrument.

CROSS-REFERENCE TO RELATED APPLICATION(S)

This application is a continuation of U.S. patent application Ser. No. 13/844,324 filed on Mar. 15, 2013, which is hereby incorporated by reference in its entirety.

TECHNICAL FIELD

The present disclosure relates generally to medical systems and, more particularly, to visualization systems, spinal decompression instruments, treatment systems, and methods for treating the spine.

BACKGROUND

Spinal nerve compression can be caused by narrowing of the spinal canal associated with arthritis (e.g., osteoarthritis) of the spine, degeneration of spinal discs, and thickening of ligaments. Arthritis of the spine often leads to the formation of bone spurs which can narrow the spinal canal and press on the spinal cord. In spinal disk degeneration, inner tissue of the disk can protrude through a weakened fibrous outer covering of the disk. The bulging inner tissue can press on the spinal cord and/or spinal nerve roots. Ligaments located along the spine can thicken over time and press on the spinal cord and/or or nerve roots. Spinal nerve compression can cause lower back pain, hip pain, and leg pain and may also result in numbness, depending on the location of the compressed nerve tissue. In the lower back, spinal stenosis may lead to spinal cord compression and numbness of the legs. Unfortunately, it may be difficult to treat spinal nerve compression without injuring or traumatizing non-targeted tissue.

BRIEF DESCRIPTION OF THE DRAWINGS

The same reference numerals refer to like parts or acts throughout the various views, unless otherwise specified.

FIG. 1 is a side view of a visualization system in accordance with an embodiment of the disclosure.

FIG. 2 is a side view of a visualization instrument protecting a spinal cord in accordance with an embodiment of the disclosure.

FIG. 3 is an enlarged superior view of tissue adjacent to a vertebral foramen and the visualization instrument positioned between a ligamentum flavum and dura sac.

FIG. 4 is a flowchart illustrating a method for reducing spinal nerve compression in accordance with one embodiment of the disclosure.

FIGS. 5-8 illustrate various stages of a procedure for reducing spinal nerve compression in accordance with one embodiment of the disclosure.

FIG. 9 is a superior anatomical view of a visualization instrument positioned using a transforamonal approach in accordance with an embodiment of the disclosure.

FIG. 10 is an enlarged view of the visualization instrument of FIG. 9 adjacent to the spinal cord in accordance with one embodiment of the disclosure.

FIG. 11 is a superior anatomical view of a visualization instrument positioned using a lateral approach in accordance with an embodiment of the disclosure.

FIG. 12 is an enlarged view of the vertebral foramen of FIG. 11 with the visualization instrument positioned between the spinal cord and the ligamentum flavum.

FIG. 13 is a side view of a distal portion of a visualization instrument positioned within a dura sac in accordance with an embodiment of the disclosure.

FIG. 14 is a superior anatomical view of the vertebral foramen of FIG. 13 in accordance with an embodiment of the disclosure.

FIG. 15 is a side view of a visualization system and a treatment system positioned at different levels along a spine in accordance with an embodiment of the disclosure.

FIG. 16 is a side view of the visualization system and the treatment system of FIG. 15 with the spine shown in cross-section.

FIGS. 17-19 are side views of a visualization instrument and treatment system positioned along a spine.

FIG. 20 is a side view of the visualization instrument in accordance with an embodiment of the disclosure.

FIG. 21 is a plan view of the visualization instrument of FIG. 20.

FIG. 22 is a side view of a distal portion of the visualization instrument of FIG. 20 positioned between the ligamentum flavum and the spinal cord in accordance with an embodiment of the disclosure.

FIG. 23 is an isometric view of a visualization instrument in accordance with an embodiment of the disclosure.

FIG. 24 is a plan view of a visualization instrument capable of delivering contrast media in accordance with an embodiment of the disclosure.

FIG. 25 is a plan view of a visualization instrument with the deployable media delivery element in accordance with an embodiment of the disclosure.

FIG. 26 is a plan view of the delivery element of FIG. 25 in a deployed position.

DETAILED DESCRIPTION

The following disclosure describes various embodiments in medical systems, instruments, devices, and associated methods of use. At least some embodiments include a visualization instrument that can be viewed to assist in a spinal procedure. Visualization techniques can be used to view at least a portion of a treatment instrument (e.g., a distal tip of a tissue removal instrument) and at least a portion of the visualization instrument to perform the procedure. Certain details are set forth in the following description and in FIGS. 1-26 to provide a thorough understanding of such embodiments of the disclosure. Other details describing well-known structures and systems often associated with, for example, visualization, treating the spine, spinal nerves (e.g., nerves in the spinal cord, nerves in nerve roots exiting the spinal cord, etc.), or decompression procedures are not set forth in the following description to avoid unnecessarily obscuring the description of various embodiments of the disclosure.

The terms “distal” and “proximal” within this description, unless otherwise specified, reference a relative position of the portions of a system, instruments, and/or associated delivery devices with reference to an operator and/or a location in the patient. For example, in referring to visualization instruments described herein, the term “proximal” can refer to a position closer to the operator, and the term “distal” can refer to a position that is more distant from the operator.

A. Overview

At least some visualization instruments disclosed herein can be used to identify features, such as targeted tissue and non-targeted tissue, and/or used as a point of reference to position other instruments and tools. In some embodiments, a visualization instrument can be positioned to protect the spinal cord and define a working space. A series of treatment instruments can be moved within the working space to crush, separate, cut, debulk, break, fracture, remove, or otherwise alter tissue at a treatment site. If the treatment instruments move towards the spinal cord, the visualization instrument can serve as a working barrier to inhibit or prevent injury and/or trauma to the spinal cord.

At least some embodiments are methods for treating a subject (e.g., a human subject). The methods include positioning a tissue protector of a visualization instrument in an epidural space. The tissue protector can be viewed via fluoroscopy to identify margins of the epidural space, dura, ligamentum flavum, nerve roots, and/or other tissue. The wide range of different types of fluoroscopy (e.g., anterior posterior imaging, lateral imaging, contralateral oblique imaging, etc.) can be used to view the visualization instrument, as well as treatment tools or delivery devices used to perform a procedure.

At least some embodiments are methods for performing a procedure on a subject and include positioning a distal portion of a visualization instrument in a vertebral column of the subject. Another instrument (e.g., a treatment instrument) can be positioned while viewing both the treatment instrument and a distal portion of the visualization instrument under, for example, fluoroscopy. A spinal decompression procedure can be performed using the treatment instrument. In one embodiment, the visualization instrument can be a radiopaque epidural catheter having a flexible elongated main body. In some procedures, the epidural catheter can be moved along the vertebral column through any number of vertebrae. In other embodiments, the visualization instrument is a catheter configured to be positioned within the dura sac or other suitable location. Such catheters can have a relatively low profile. An opening, if any, defined by, and laterally adjacent to, the distal portion can be smaller than a distal head or tool portion of the treatment instrument. As such, the distal head of the treatment instrument is prevented from contacting non-target tissue. In some embodiments, the visualization instrument includes an elongate radiopaque wire. The wire can extend from a distal end of the visualization instrument to a proximal end of the visualization instrument.

In some embodiments, a method for positioning an instrument in a subject comprises moving the tissue protector of the visualization instrument through a subject. The tissue protector can be moved from a delivery configuration to a deployed configuration to define a working space. A decompression procedure can be performed at the treatment site while viewing the deployed tissue protector. When using a treatment instrument at the working space, the treatment instrument and non-targeted tissue can be kept on opposite sides of the tissue protector.

In yet other embodiments, a method for performing a procedure on a subject includes positioning a tissue protector of a visualization instrument in an epidural space of a subject. A treatment instrument can be moved between a first vertebra and a second vertebra while the tissue protector remains in the epidural space and viewed via fluoroscopy. A physician can view both the treatment instrument and the tissue protector before, during, and after performing a procedure using the treatment instrument.

In some embodiments, a treatment system for treating spinal compression comprises a visualization instrument including a tissue protector configured to be positioned in an epidural space and viewed using a fluoroscopy. The treatment system can further include a treatment instrument configured to perform a decompression procedure at a treatment site while the tissue protector prevents access to the spinal cord. In some embodiments, the tissue protector can cover a posterior region of the spinal cord facing a treatment site.

B. Visualization Systems, Visualization Procedures, and Decompression Procedures

FIG. 1 is a side view of a visualization system 100 in accordance with one embodiment of the disclosure. The visualization system 100 includes a visualization instrument 110 and a delivery device in the form of a cannula 120. The cannula 120 extends through a subject's skin 140, subcutaneous tissue 142, and a supraspinal ligament 150. The visualization instrument 110 extends through the cannula 120 and along a spinal or vertebral column 123.

FIG. 2 is a detailed side view of a portion of the visualization system 100. Vertebra 170, 174 are shown in cross section. FIG. 3 is a detailed superior anatomical view of a spinal canal 200. Referring to FIGS. 2 and 3 together, the visualization instrument 110 includes a distal portion 163 positioned between a ligamentum flavum 194 and a spinal cord 180. The spinal cord 180 is positioned between the ligamentum flavum 194 and a ligament 198 and extends from the brain to the bottom of the spine. Spinal nerves branch from the spinal cord 180, exit the spine, and extend to the parts of the body.

The distal portion 163 is viewable using, for example, fluoroscope, MR imaging, CT imaging, or other suitable imaging techniques. By viewing the distal portion 163, a physician can conveniently identify the location and/or margins of the spinal cord 180 and ligamentum flavum 194. The distal portion 163 can be moved to different positions to identify targeted or non-targeted tissue, which can include, without limitation, the ligamentum flavum 194, the spinal cord 180, the ligament 198, nerves branching from the spinal cord 180, vertebrae 170, 174, and other features or anatomical structures proximate to the spine. The distal portion 163 can include a tissue protector 190 (e.g., a section of the distal portion 163) configured to inhibit, limit, or substantially prevent damage and/or injury to the spinal cord 180 and can define a working space 127 (FIG. 2).

FIG. 4 is a flow chart illustrating a method 301 for visualizing and performing spinal nerve decompression in accordance with an embodiment of the disclosure. At stage 300, a delivery device can provide access to a treatment site. At stage 302, a visualization instrument can be positioned using fluoroscopy. At stage 304, one or more treatment instruments can be delivered to a working space defined, at least in part, by a tissue protector of the visualization instrument. At stage 305, a spinal procedure can be performed. The spinal procedure (including posterior lumbar decompression procedures) can involve altering tissue, implanting devices, or other procedures for treating various spine conditions. Tissue can be altered by cutting tissue, loosening tissue, crushing bone, or otherwise disrupting tissue at a treatment site. In some decompression procedures, tissue can be removed from one or more lateral recesses of a vertebra. In other decompression procedures, tissue can be removed from the spinal cord, vertebrae, or other site along the spine, as discussed in connection with FIGS. 8-19 and 22.

FIGS. 5-8 illustrate various stages of a procedure in accordance with one embodiment of the disclosure. Referring now to FIG. 5, the cannula 120 can be delivered using a posterior midline approach. An incision can be made in the supraspinal ligament 150 and the cannula 120 can be passed through the incision until it is inserted between spinous processes 240, 244. A distal end 252 of the cannula 120 can be positioned within an interspinous space 261. Delivery sheaths, delivery catheters, access ports, or other types of delivery devices can also be used to provide access to the treatment site. The distal portion 163 can be inserted into a proximal end 250 of the cannula 120, moved along a passageway of the cannula 120, and delivered out of the distal end 252. The distal portion 163 can be moved in the anterior direction through the interspinous space 261, through the ligamentum flavum, and into the epidural space (or other desired location).

FIG. 6 shows the visualization instrument 110 including the main body 280 and a proximal portion 269 positioned outside of the subject. The proximal portion 269 can include a steering assembly 270 used to steer the visualization instrument 110 by, for example, operating control elements 272, 274. One or more pull wires, pull rods, or other components can extend through the main body 280 and can be coupled to the distal end of the visualization instrument 110. The control elements 272, 274 can be levers, dials, or other elements that can be manipulated to bend, rotate, displace, or otherwise move the instrument 110. In other embodiments, the visualization instrument 110 may not have steering capability. A delivery device can be used to guide such visualization instruments to a desired site.

FIGS. 7 and 8 show a treatment instrument 299 that has been delivered through the cannula 120 and positioned at the working space 127. One or more markers (one marker 197 is shown in FIG. 8) can be used to identify the spinal cord 180 and can serve as a reference point to position the treatment instrument 299. However, markers can also be located on the exterior surface of the main body 280 and/or tissue protector 190, within the main body 280 and/or tissue protector 190, or at other suitable locations. Markers can include, without limitation, an array of radiopaque markers made of radiopaque materials, such as metals, radiopaque polymers, or the like. The radiopaque markers can be evenly or unevenly spaced apart along the length of the tissue protector 190. In other embodiments, the entire main body 280 and distal portion 193 can be made of radiopaque material. For example, the main body 280 and tissue protector 190 can be a flexible metal wire (e.g., an elongate radiopaque wire) or a bundle of flexible metal wires.

Referring to FIG. 8, a longitudinal axis 191 of the tissue protector 190 is oriented in the superior-inferior direction and is generally parallel to the long axis of the spinal cord 180. Additionally, the axis 191 can be generally perpendicular to the portion of the main body 280 extending in posterior-anterior direction. The ligamentum flavum 194 and spinal cord 180 can snugly hold the tissue protector 190 to help minimize movement of the instrument 110, even if the instrument 299 contacts the main body 280. An atraumatic tip 314 can be moved in the superior direction (indicate by arrow 316) to position most of the tissue protector 190 within the vertebral canal 200, but it can be located at other locations. In some embodiments, the tissue protector 190 can made of a compliant material (e.g., silicon, rubber, elastomers, etc.) to cushion tissue. In other embodiments, the tissue protector 190 can be made of a rigid or semi-rigid materials to distribute pressure to a large area of tissue.

FIG. 8 shows the instrument 299 having a working or distal portion 307 configured to break, cut, scrape, crush, or otherwise alter target tissue at the treatment site 263. The target tissue can include, without limitation, bone (e.g., lamina, bone of lateral recesses, facets, including inferior facets, etc.), bone spurs (e.g., bone spurs associated with osteoarthritis), tissue bulging from discs, tissue of thickened ligaments, spinal tumors, displaced tissue (e.g., tissue displaced by spinal injury), or other tissue that may cause or contribute to spinal nerve decompression. In procedures treating stenosis, the distal portion 307 can be used to remove tissue associated with central canal stenosis, lateral recess stenosis, or other types of stenosis.

If the distal portion 307 is moved in the anterior direction (indicated by arrow 310) the tissue protector 190 can physically block the distal portion 307. The distal portion 307 can also be inserted into the vertebral canal 200 without injuring or traumatizing the spinal cord 180. As a result, the instrument 299 can be safely moved throughout the working space 127. The shape and configuration of the tissue protector 190 can be selected based on the configuration of the distal portion 307. For example, the tissue protector 190 can be large enough to ensure that exposed regions, if any, of the spinal cord 180 (i.e., the regions of the spinal cord 180 accessible via the interspinous space 313) are smaller than the distal portion 307.

The treatment instrument 299 can be, without limitation, a surgical instrument (e.g., a scalpel), scraping instrument, cutting instrument, or other instrument or tool for altering tissue. U.S. Patent Application No. 61/755,392, filed on Jan. 22, 2013, discloses various types of surgical instruments that can be used in, or incorporated into, the systems and methods disclosed herein. Such instruments include, but are not limited to, debulker instruments, tissue removal instruments, cutting instruments, and debulker instruments and other systems, instruments, and devices disclosed in U.S. Application No. 61/755,329, which is incorporated by reference in its entirety.

To help position the distal portion 307, both the distal portion 307 and the tissue protector 190 can be viewed using, for example, fluoroscopy. The tissue protector 190 can serve as a reference point to help the physician identify critical areas of non-targeted tissue and/or assist in positioning of the distal portion 307. In some procedures, the tissue protector 190 can remain substantially stationary while the distal portion 307 is used to perform a procedure at the treatment site 263, although the tissue protector 190 can be repositioned any number of times during a treatment session.

After completing the procedure, the instrument 299 can be removed from the subject. The visualization instrument 110 and the cannula 120 can then be removed from the subject without injuring and/or traumatizing tissue.

FIGS. 9 and 10 show a visualization instrument 292 positioned using a transforaminal approach. The visualization instrument 292 can include a distal portion 294 with a tissue protector 293 extending laterally about the spinal cord 180 to provide a wide working space. An operator can grip the proximal portion 297 positioned outside of the subject to reposition the tissue protector 293. Treatment instruments or tools can be delivered using a transforaminal approach to perform decompression procedures at, for example, the lateral recesses. The tissue protector 293 can have a generally rectangular shape, partially cylindrical shape, or other shape or configuration suitable for overlaying the spinal cord 180.

Visualization instruments can be delivered using other access techniques. For example, FIGS. 11 and 12 show a visualization instrument 303 positioned using a lateral approach and having a distal portion 311 with a tissue protector 309 overlaying the posterior region of the dura sac 181. FIG. 12 shows the tissue protector 309 adjacent to opposing sides 500, 502 of the ligamentum flavum 194. In some embodiments, the tissue protector 309 wraps around most of the circumference of the spinal cord 180 to protect the dura sac 181 when performing decompression procedures at the lateral-most regions of the vertebral foramen 503. An operator can use a handle 317 (FIG. 11) at the proximal portion 315 (FIG. 11) to manually reposition the tissue protector 309.

FIGS. 13 and 14 show a visualization instrument 402 that includes a distal portion 401 with a tissue protector 403 positioned within dura sac 181. Referring to FIG. 13, the tissue protector 403 spans a gap 209 between the vertebra 170, 174. As such, the entire length of the spinal cord 180 positioned between the vertebra 170, 174 is protected. Other visualization instruments can also be positioned within the spinal cord 180. For example, the visualization instrument 110 of FIGS. 1 and 2 can be inserted into the dura and moved in the anterior or superior direction. To perform a myelogram, such instrument can have a port capable of delivering contrast media directly into the spinal cord 180.

Referring now to FIG. 14, the tissue protector 403 is positioned between the dura sac 181 and spinal nerves 405. If a treatment instrument or tool punctures the dura sac 181, the tissue protector 403 can shield the spinal nerves 405. Multiple visualization instruments can be used together in a single procedure. In one procedure, the visualization instrument 402 can be used to protect spinal nerves 405 while another visualization instrument, such as the visualization instrument 110 of FIGS. 1 and 2, protects the dura sac 181.

FIG. 15 is a side view of a visualization instrument 610 and a treatment system 612 in accordance with an embodiment of the disclosure. FIG. 16 is a detailed side view of portions of the visualization instrument 610 and treatment system 612. The spine 121 is shown in cross-section in FIG. 16. The visualization instrument 610 extends through an interspinous space 613 and its main body 620 extends through the vertebral canal 629 (FIG. 16). A tissue protector 690 can extend along the spinal canal 621 to a location superior to the treatment site. In FIG. 16, the treatment site is between the spinous processes 450, 451, so the tissue protector 690 can extend from a first level 660 to an adjacent level 661, thereby spanning a gap 340 (FIG. 16).

Referring again to FIG. 15, the treatment system 612 can include a delivery device in the form of a cannula 644, an instrument 619, and an implantable device 710. The implantable device 710 can be an interspinous spacer, fixation device, plate, or other type of spinal implant. One suitable such implantable device is the Superion® interspinous spacer from VertiFlex, Inc. or other similar device. The implantable device 710 can be implanted while imaging the device 710 and the tissue protector 690 and can be delivered via a midline approach, a transforaminal approach, an ipsilateral approach, or a lateral approach. The implantable device 710 can be deployed to engage, and couple to, the spinous processes 450, 451 to, for example, reduce or eliminate spinal compression, pain, or combinations thereof. Throughout the deployment process, the spinal cord 180 is protected by the tissue protector 190.

After implanting the device 710, the treatment system 612 can be removed from the subject. The visualization instrument 610 can be pulled proximally through the cannula 120 and removed from the subject. The visualization instrument 610 and treatment system 612 can be used to treat other locations along the spine.

FIG. 17 shows a visualization instrument 800 entering the spine at the lumbar region 810. A treatment instrument 820 can perform a procedure at the thoracic region 812 while a tissue protector 833 (shown in phantom) protects non-targeted tissue at the thoracic region 812. The visualization instrument 800 can be a catheter (e.g., a radiopaque epidural catheter or other instrument disclosed herein). FIG. 18 shows the visualization instrument 800 accessing the spine or vertebral column at the thoracic region 812 to protect non-targeted tissue at the lumbar region 810. FIG. 19 shows the visualization instrument 800 positioned at the sacral region 850 to perform a procedure at another level. Because the tissue protectors disclosed herein can be conveniently moved along the spine, the tissue protectors can be inserted at an access that is separated from the treatment site by one or more vertebrae. Accordingly, the access site can be at the cervical region, thoracic region, lumbar region, or sacral region to perform a procedure at treatment site at the cervical region, thoracic region, lumbar region, or sacral region.

FIG. 20 is a side view of a visualization instrument 900 that includes a distal portion 901, a proximal portion 903, and a main body 905. The distal portion 901 includes a tissue protector 902 in accordance with an embodiment of the disclosure. FIG. 21 is a plan view of the tissue protector 902 that includes protective arms 912 (individually 912 a, 912 b, 912 c, 912 d, 912 e, 912 f in FIG. 21) movable from a delivery configuration 917 (shown in phantom line in FIG. 20) to the deployed configuration 919. To deliver the tissue protector 902, the arms 912 can be in the delivery configuration 917 for delivery through a cannula or other delivery device. As the tissue protector 902 exits the cannula, the arms 912 to move from the delivery configuration to the deployed configuration, as indicated by arrow 924, 926. In some embodiments, the arms 912 are biased outwardly and can self-deploy. In other embodiments, the arms 912 can be deployed using one or more balloons, pull rods, pull wires, or other component for providing controlled movement of the arms 912.

Referring to FIG. 21, the arms 912 can be generally evenly spaced apart from one another and made of metal, plastic, or other material capable of withstanding contact with a treatment instrument so as protect adjacent tissue. In some embodiments, a protective or shielding member 920 (shown in phantom line) can be carried by the arms 912 and can include, without limitation, a mesh, a net, a sheet (single layer or multilayer layer sheet), drapable fabric, a plate, or other protective barrier (i.e., a barrier for preventing injury or trauma to tissue) that can assume different configurations by expanding, unfurling, or the like. The protective member 920 can have a wide range of shapes and configurations, including a generally circular shape, spherical shape, rectangular shape, or the like.

FIG. 22 shows the tissue protector 902 in the deployed configuration. Tips 930 of the arms 912 can be positioned within vertebral canals 200, 204 to protect the entire length of the spinal cord 180 exposed by the interspinous space 911. In some embodiments, the entire portion of the spinal cord 180 accessible via the interspinous space 911 is covered by the protective member 920 to prevent puncturing of the dura sac 181, while the arms 912 can help withstand significant forces from treatment instruments. Accordingly, the arms 912 and protective member 920 can work together to provide enhanced protection.

FIG. 23 is an isometric view of a visualization instrument 1100 including a tissue protector 1102 in accordance with another embodiment of the disclosure. The tissue protector 1102 is movable from a delivery configuration 1110 (shown in phantom line) to the deployed configuration 1112. The tissue protector 1102 can include an inflatable member (e.g., a single chamber balloon, a multi-chamber balloon) that can be inflated with a fluid to provide cushion to further inhibit or prevent tissue trauma and/or injury. Such inflatable members can be made of a highly compliant material, including, without limitation, silicon, rubber, elastomers, or the like. One or more markers can be positioned along the exterior surface or within the tissue protector 1102. The inflation fluid can be visualization media (e.g., contrast media) in the form of a flowable radiopaque substance (e.g., a radio contrast agent, barium sulfate solution, or the like) or other viewable substance. Non-ionic contrast media can be used if the tissue protector 1102 is positioned within the dura sac. As a result, the inflation fluid can provide both cushioning and visualization functionality.

FIG. 24 is an elevational view of a visualization instrument 1200 that includes a distal portion 1201, a proximal portion 1203, and a main body 1205 therebetween. The distal portion 1201 includes a tissue protector 1211 having deployable elements 1204, 1204 movable from a delivery configuration inside the body 1205 to the illustrated deployed configuration. Visualization media can be delivered out of a port 1220 for additional imaging. To perform an epidurogram, the visualization media can be delivered out of the port 1220 when the tissue protector 1211 is positioned in the epidural space. The members 1202, 1204 can be deployed before, during, or after delivery of the Visualization media. Other visualization instruments disclosed herein can also include one or more ports for delivering media.

FIG. 25 is a side elevational view of a visualization instrument 1300 in accordance with an embodiment of the disclosure. FIG. 26 is a side view of the visualization instrument 1300. Referring to FIG. 25, the visualization instrument 1300 includes a distal portion 1301, a proximal portion 1303, a main body 1305, and a media delivery element 1320 in an undeployed position. In some embodiments, the media delivery element 1320 can be housed within a lumen 1321. Referring to FIG. 26, the delivery element 1320 can be moved out of an aperture 1330 to deliver media.

In myelography procedures, a tissue protector 1333 can moved along the epidural space adjacent to the dura. The delivery element 1302 can be moved out of the aperture 1330, which faces the dura, to puncture the dura sac. After an end 1329 is within the dura, visualization media (e.g., a non-ionic contrast media) can be delivered directly into the spinal fluid surrounding the spinal cord. The delivery element 1320 can be positioned under fluoroscopic guidance to ensure that spinal nerves are not damaged or injured. After delivering the media, the delivery element 1302 can be drawn back into the main body 1323. As such, the media can be kept outside of the epidural space and localized within the dura. Myelography can provide detailed images (i.e., myelograms) of the spinal cord, thecal sac, nerve tissue (including nerve roots), or other features of interest. Additionally, myelography procedures can provide enhanced viewing of non-targeted structures (e.g., dura), and nerve roots compared to epidurography procedures. For example, visualization media of a myelography procedure may travel (e.g., via controlled leakage) to nerve roots to visualize the nerve roots when removing bone of the neural foramen. In some embodiments, myelography visualization media can be used to verify decompression of the spinal cord because the dura can move outwardly to confirm that the pressure applied to the spinal cord is decreased or eliminated. If the dura is damaged (e.g., tears, leaks, or the like), myelography visualization media can escape out of the damaged region of the dura. A physician can view the leakage to confirm that the dura has been damaged, as well as identifying the location of the damage. The physician can then repair the dura or otherwise alter the surgical procedure. Accordingly, myelography visualization media can be used to provide useful real-time feedback. Other visualization instruments disclosed herein can have delivery elements similar to the delivery element 1302 discussed in connection with FIGS. 25 and 26 in order to deliver contrast media (or other media) into tissue. For example, the tissue protector 190 of FIG. 2 can have a deployable delivery element.

Although many embodiments discussed herein are discussed in the context of fluoroscopy, other visualization techniques can be used to view treatment instruments and/or visualization instruments to identify targeted features, treatment sites, and/or non-targeted features. Treatment instruments and/or visualization instruments can be viewed when altering tissue and/or delivering a spinal device, such as a spinal implant, a spacer device, prosthetics disk, or the like. In certain procedures, visualization instruments disclosed herein can be used to identify margins of the epidural space, dura, ligamentum flavum, and/or nerve roots relative to the lamina and interlaminar space, as well as the features of instruments.

The visualization instruments disclosed herein can be located at other locations to protect other non-target tissue. Other embodiments can include tissue protectors specifically designed to protect portions of the vertebrae, nerve roots, or other structures near the spine. Additionally, multiple visualization instruments can cooperate to simultaneously protect tissue while also serving as reference points under visualization.

CONCLUSION

The above detailed descriptions of embodiments of the technology are not intended to be exhaustive or to limit the technology to the precise form disclosed above. Although specific embodiments of, and examples for, the technology are described above for illustrative purposes, various equivalent modifications are possible within the scope of the technology, as those skilled in the relevant art will recognize. For example, while steps are presented in a given order, alternative embodiments may perform steps in a different order. The various embodiments described herein may also be combined to provide further embodiments. For example, features from various instruments can be combined with features and methods disclosed in U.S. Pat. No. 8,012,207; U.S. Pat. No. 8,123,807; U.S. Pat. No. 8,152,837, and U.S. application Ser. No. 12/217,662 (U.S. Publication No. 2008/0287997) which are incorporated by reference in their entireties. U.S. Provisional Application Nos. 61/639,828, 61/745,470, and 61/755,329, which are hereby incorporated by reference herein and made a part of this application. A wide range of treatment instruments can be used to address a wide range of symptoms, conditions, and/or diseases, including, without limitation, spinal nerve compression (e.g., spinal cord compression, spinal nerve root compression, or the like), spinal disk herniation, osteoporosis, stenosis, or other diseases or conditions. In one embodiment, the system 100 is used to perform a spinal cord decompression procedure, which can include removing bone from one or more vertebrae, separating the ligamentum flavum from one or more vertebrae, cutting or debulking the ligamentum flavum, and/or removing loose tissue.

Where the context permits, singular or plural terms may also include the plural or singular term, respectively. Moreover, unless the word “or” is expressly limited to mean only a single item exclusive from the other items in reference to a list of two or more items, then the use of “or” in such a list is to be interpreted as including (a) any single item in the list, (b) all of the items in the list, or (c) any combination of the items in the list. Additionally, the term “comprising” is used throughout to mean including at least the recited feature(s) such that any greater number of the same feature and/or additional types of other features are not precluded. It will also be appreciated that specific embodiments have been described herein for purposes of illustration, but that various modifications may be made without deviating from the technology. Further, while advantages associated with certain embodiments of the technology have been described in the context of those embodiments, other embodiments may also exhibit such advantages, and not all embodiments need necessarily exhibit such advantages to fall within the scope of the technology. Accordingly, the disclosure and associated technology can encompass other embodiments not expressly shown or described herein. 

1.-19.
 21. A treatment system for treating spinal compression of a subject, comprising: a delivery cannula; a visualization instrument including a tissue protector and an elongate body, the tissue protector is configured to be positioned in an epidural space and viewed using fluoroscopy while the elongate body extends through the delivery cannula and out of the subject; and a treatment instrument configured to perform a decompression procedure at a treatment site while the tissue protector prevents access to the spinal cord and the elongate body extends through the delivery cannula.
 22. The treatment system of claim 21, wherein the delivery cannula has an open distal end configured to be positioned between adjacent spinous processes of adjacent vertebrae.
 23. The treatment system of claim 21 wherein the tissue protector includes a plurality of deployable arms for protecting tissue while the treatment instrument is used to perform at least a portion of the decompression procedure.
 24. The treatment system of claim 21 wherein the visualization instrument includes a tissue protector comprising one or more balloons, nets, and sheets.
 25. The treatment system of claim 21 wherein the visualization instrument includes at least one radiopaque marker.
 26. The treatment system of claim 21 wherein the treatment instrument is configured to remove bone from a vertebral column of the subject, separating a portion of a ligamentum flavum from at least one vertebra of the subject, and/or remove a portion of the ligamentum flavum from the subject. 